Canonical Allele Identifier: CA2320962375
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527564A= , CM000681.2:g.7527564A= GRCh38
NC_000019.9:g.7592450A= , CM000681.1:g.7592450A= GRCh37
NC_000019.8:g.7498450A= NCBI36
NG_015806.1:g.9955A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.616A= MANE Select ENSP00000264079.5:p.Ser206=
ENST00000264079.10:c.616A= ENSP00000264079.5:p.Ser206=
ENST00000394321.9:n.696A=
ENST00000598406.1:n.437A=
ENST00000601003.1:c.572-300A= ENSP00000469074.1:n.572-300A=
NM_020533.2:c.616A= NP_065394.1:p.Ser206=
NM_020533.3:c.616A= MANE Select NP_065394.1:p.Ser206=